4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID

4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID
  • CAS No.:2510-32-9
Other grades of this product :
4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID Basic information
Product Name:4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID
Synonyms:4-METHYL-5-OXAZOLECARBOXYLIC ACID;4-METHYL-OXAZOLE-5-CARBOXYLIC ACID;4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID;4-methyl-1,3-oxazole-5-carboxylic acid(SALTDATA: FREE);4-Methyl-1,3-oxazole-5-carboxylic acid ,97%;4-Methyl-1,3-oxazole-5-carboxylic acid 95%;5-Oxazolecarboxylic acid, 4-Methyl-;4-Methyl-oxazol-5-carboxylic acid
CAS:2510-32-9
MF:C5H5NO3
MW:127.1
EINECS:
Product Categories:Carboxylic Acids;Oxazoles, Isoxazoles & Benzoxazoles;Heterocyclic Compounds;Carboxylic Acids;Oxazoles, Isoxazoles & Benzoxazoles;Building Blocks;Heterocyclic Building Blocks;Oxazoles
Mol File:2510-32-9.mol
4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID Chemical Properties
Melting point 239 °C
Boiling point 267.3±20.0 °C(Predicted)
density 1.348±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
pka2.09±0.31(Predicted)
form powder to crystal
color White to Gray to Brown
InChIKeyZIXUNDOOBLSXPE-UHFFFAOYSA-N
CAS DataBase Reference2510-32-9
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-36/37/38
Safety Statements 22-26-36/37/39
WGK Germany 3
Hazard Note Irritant
HS Code 29349990
MSDS Information
4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID Usage And Synthesis
Chemical PropertiesWhite to tan solid
Uses4-Methoxyoxazole-5-carboxylic Acid is used in the synthesis of highly selective α4β2-Nicotinic acetylcholine receptor agonists used in the treatment of cognitive disorders. It is also used in the synthesis of small molecule human FPR1 receptor antagonists.
UsesUsed in a palladium-catalyzed cross-coupling between heteroaryl carboxylic acids and aryl bromides leading to arylated heterocycles.
4-METHYL-1,3-OXAZOLE-5-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Hydrochloric acid-->Ethyl acetate-->Diethyl ether-->Potassium carbonate-->Formic acid-->Ammonium formate-->Ethyl 2-chloroacetoacetate

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